Chiral Iridium(III) Complexes in Light-Emitting Electrochemical Cells: Exploring the Impact of Stereochemistry on the Photophysical Properties and Device Performances
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide Despite hundreds of cationic bis-cyclometalated iridium(III) complexes having been explored as emitters for light-emitting electrochemical cells (LEECs), uniformly their composition has been in the form of a racemic mixture of Λ and Δ enantiomers. The investigation of LEECs using enantiopure iridium(III) emitters, however, remains unprecedented. Herein, we report the preparation, the crystal structures, and the optoelectronic properties of two families of cyclometalated iridium(III) complexes of the form of [(C^N) 2 Ir(dtBubpy)]PF 6 (where dtBubpy is 4,4′-di- tert -butyl-2,2′-bipyridine) in both their racemic and enantiopure configurations. LEEC devices using Λ and Δ enantiomers as well as the racemic mixture of both families have been prepared, and the device performances were tested. Importantly, different solid-state photophysical properties exist between enantiopure and racemic emitters, which are also reflected in the device performances.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Light-Emitting Diodes Research · Lanthanide and Transition Metal Complexes · Magnetism in coordination complexes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Organic Semiconductor Centre, EaStCHEM School of Chemistry, University of St Andrews, St Andrews, Fife KY16 9ST, United Kingdom
Instituto de Ciencia Molecular, Universidad de Valencia, c/Catedrático J. Beltrán, 2, Paterna 46980, Spain
Funding
University of St Andrews
References (41)
Show source-provided references
1. 10.1002/anie.20120147110.1002/anie.201201471 ↗
2. 10.1021/ja012721j10.1021/ja012721j ↗
3. 10.1021/ja034522110.1021/ja0345221 ↗
4. 10.1039/c2jm16185k10.1039/c2jm16185k ↗
5. 10.1016/j.mattod.2014.04.02910.1016/j.mattod.2014.04.029 ↗
6. 10.1002/chem.20060061810.1002/chem.200600618 ↗
7. 10.1002/ejic.20130084910.1002/ejic.201300849 ↗
8. 10.1039/B812281D10.1039/B812281D ↗
9. 10.1021/ic050970t10.1021/ic050970t ↗
10. 10.1002/ejic.20130041110.1002/ejic.201300411 ↗
11. 10.1002/ejic.20150008710.1002/ejic.201500087 ↗
12. 10.1039/C5DT03642A10.1039/C5DT03642A ↗
13. 10.1002/jssc.20060040910.1002/jssc.200600409 ↗
14. 10.1002/chem.20090265210.1002/chem.200902652 ↗
15. 10.1016/j.ica.2008.10.01110.1016/j.ica.2008.10.011 ↗
16. 10.1021/ja048655d10.1021/ja048655d ↗
17. 10.1021/ic700494e10.1021/ic700494e ↗
18. 10.1021/ja067016v10.1021/ja067016v ↗
19. 10.1039/b311693j10.1039/b311693j ↗
20. 10.1039/c1dt10588d10.1039/c1dt10588d ↗
21. 10.1021/ic701747j10.1021/ic701747j ↗
22. 10.1016/j.chroma.2016.05.05910.1016/j.chroma.2016.05.059 ↗
23. 10.1039/a705947g10.1039/a705947g ↗
24. 10.1039/b703761a10.1039/b703761a ↗
25. 10.1021/ja309031h10.1021/ja309031h ↗
26. 10.1021/acs.inorgchem.5b0191010.1021/acs.inorgchem.5b01910 ↗
27. 10.1002/chem.20120070910.1002/chem.201200709 ↗
28. 10.1002/ejic.20160026010.1002/ejic.201600260 ↗
29. 10.1021/cm401077310.1021/cm4010773 ↗
30. 10.1039/C5QI00177C10.1039/C5QI00177C ↗
31. 10.1039/C6TC00151C10.1039/C6TC00151C ↗
32. 10.1039/C6DT02619B10.1039/C6DT02619B ↗
33. 10.1021/ic100521t10.1021/ic100521t ↗
34. 10.1021/cm301171610.1021/cm3011716 ↗
35. 10.1021/j100820a00910.1021/j100820a009 ↗
36. 10.1021/cm050314r10.1021/cm050314r ↗
37. 10.1021/cm071337410.1021/cm0713374 ↗
38. 10.1016/j.orgel.2014.12.02810.1016/j.orgel.2014.12.028 ↗
39. 10.1039/C4TC01171F10.1039/C4TC01171F ↗
40. 10.1039/c2jm33969b10.1039/c2jm33969b ↗
41. 10.1039/C4SC03942D10.1039/C4SC03942D ↗